Search

everythinglearnresearchcommunity

for

Search:↓

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Korean long-tailed chickens have unique genes valuable for ornamental breeding.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Humans have ancient DNA from Neanderthals and other lineages in their chromosomes, affecting traits and evolution.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

Pubic hair is thicker than axillary and scalp hair, useful for forensic identification.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

A truncated protein linked to breast cancer may change cell adhesion.

Gene variation affects prostate issues and hair loss.

Planarians regenerate using conserved gene expression mechanisms, with runt-1 crucial for cell type specification.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

The research identified new skin traits in mice, some linked to human skin conditions.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

The guinea pig α-lactalbumin gene was successfully expressed in the mammary glands of transgenic mice.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.